ALPHA CF- aconitum napellus, bryonia alba root, eucalyptus globulus leaf, eupatorium perfoliatum flowering top, gelsemium sempervirens root, ipecac, phosphorus, tablet

Alpha CF by

Drug Labeling and Warnings

Alpha CF by is a Homeopathic medication manufactured, distributed, or labeled by Schwabe North America, Inc., Schwabe Mexico, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS:

Aconitum napellus 4X

Bryonia alba 4X

Eucalyptus globulus 2X

Eupatorium perfoliatum 6X

Gelsemium sempervirens 4X

Ipecacuanha 3X

Phosphorus 6X

INACTIVE INGREDIENT

INACTIVE INGREDIENT:

Lactose monohydrate
Magnesium stearate
Microcrystalline cellulose

DOSAGE & ADMINISTRATION

Dosage and Administration:

Directions: Sublingual medication.

Place tablet under tongue and let dissolve slowly.

Best if taken at least 15 minutes before and a half hour after eating, brushing teeth, or drinking anything except water

.

Adults and children 12 years of age and older:

 At first sign of cold or flu, take 1 tablet every hour and 2 or 3 tablets before going to sleep.

As symptoms subside, take 1 tablet every 2 or 3 hours.

Children 6 to 12:

Take 1/2 tablet every hour and 1 or 1 1/2 tablets before going to sleep.
As symptoms subside, take 1/2 tablet every 2 or 3 hours.

Children under 2:

Ask a doctor

INDICATIONS & USAGE

Indication and Usage:

Uses: Temporarily relieves these symptoms: fever, chills, sneezing, stuffed-up nose, runny nose, coughing, sore throat, headache, minor aches and pains.

WARNINGS

WARNINGS:

Sore Throat Warning: Severe or persistent sore throat for more that 2 days or if accompanied by high fever, headache, nausea, vomiting or rash may be serious.

Consult a physician promptly.

PREGNANCY OR BREAST FEEDING

Pregnancy or Breast Feeding:

If pregnant or breast-feeding, ask a healthcare professional before use.

KEEP OUT OF REACH OF CHILDREN

Children:

Keep out of the reach of children.

ASK DOCTOR

Ask a Doctor before use if you have: a persistent or chronic cough that lasts, is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema or is accompanied by excessive phlegm (mucus)

Stop use and ask a doctor if: new symptoms occur, symptoms worsen or do not get better within 7 days, fever worsens or lasts more than 3 days, cough lasts more than 7 days or occurs with rash or persisitent headache.

These could be signs of a serious condition.

OVERDOSAGE

Overdosage:

In case of overdose, seek medical help or contact a Poison Control Center immediately.

PURPOSE

Purpose:

Temporarily relieves these symptoms: fever, chills, sneezing, stuffed-up nose, runny nose, coughing, sore throat, headache, minor aches and pains.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALPHA CF 
aconitum napellus, bryonia alba root, eucalyptus globulus leaf, eupatorium perfoliatum flowering top, gelsemium sempervirens root, ipecac, phosphorus, tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53499-9339
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	4 [hp_X]
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	4 [hp_X]
EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E)	EUPATORIUM PERFOLIATUM FLOWERING TOP	6 [hp_X]
GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q)	GELSEMIUM SEMPERVIRENS ROOT	4 [hp_X]
IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L)	IPECAC	3 [hp_X]
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6)	EUCALYPTUS GLOBULUS LEAF	2 [hp_X]
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	6 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white (B;T)	Score	no score
Shape	ROUND (BT)	Size	8mm
Flavor		Imprint Code	B;T
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53499-9339-1	4 in 1 BOX	04/01/2017	12/03/2018
1		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 53499-9339-2	1 in 1 BOX	04/01/2017
2		120 in 1 BOTTLE, GLASS; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		04/01/2017

Labeler - Schwabe North America, Inc. (831153908)

Establishment
Name	Address	ID/FEI	Business Operations
Schwabe Mexico, S.A. de C.V.		812805901	manufacture(53499-9339)